A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847902



Internal ID22622837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2937279..2942943hg38UCSC Ensembl
chr12:3046445..3052109hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg385665
hg195665
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462770
Samples
Known GenesTULP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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